Canonical Allele Identifier: CA337984043

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337930C>G (hg19) ; chr1:g.2406491C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406491C>G , CM000663.2:g.2406491C>G	GRCh38
NC_000001.10:g.2337930C>G , CM000663.1:g.2337930C>G	GRCh37
NC_000001.9:g.2327790C>G	NCBI36
NG_008342.1:g.11081G>C
NG_016128.1:g.19717C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.965G>C	ENSP00000288774.3:p.Ser322Thr
ENST00000447513.7:c.905G>C MANE Select	ENSP00000407922.2:p.Ser302Thr
ENST00000650293.1:c.859G>C
ENST00000288774.7:c.965G>C	ENSP00000288774.3:p.Ser322Thr
ENST00000447513.6:c.905G>C	ENSP00000407922.2:p.Ser302Thr
ENST00000507596.5:c.905G>C	ENSP00000424291.1:p.Ser302Thr
NM_002617.3:c.905G>C	NP_002608.1:p.Ser302Thr
NM_153818.1:c.965G>C	NP_722540.1:p.Ser322Thr
XM_011541573.1:c.962G>C	XP_011539875.1:p.Ser321Thr
XM_011541574.1:c.530G>C	XP_011539876.1:p.Ser177Thr
XM_011541575.1:c.530G>C	XP_011539877.1:p.Ser177Thr
XR_946666.1:n.1021G>C
XR_946666.2:n.970G>C
NM_001374425.1:c.962G>C	NP_001361354.1:p.Ser321Thr
NM_001374426.1:c.530G>C	NP_001361355.1:p.Ser177Thr
NM_001374427.1:c.473G>C	NP_001361356.1:p.Ser158Thr
NM_002617.4:c.905G>C MANE Select	NP_002608.1:p.Ser302Thr
NM_153818.2:c.965G>C	NP_722540.1:p.Ser322Thr
NR_164636.1:n.1020G>C